Job Description
来年申請予定の製品(希少疾患)の責任者
■ 職種: 開発薬事・マネージャー
■ 会社概要:
・ 希少疾患のリーディング・カンパニー
・ パイプライン:希少疾患のパイプが複数。既に複数は販売開始されている
・ ローカルに権限移譲されているためにローカルの意向が尊重
・ 本社や海外よりも日本が先行して申請も可能
・ MRが入社したい企業のトップランク
■ 職務内容
(雇入れ直後)開発薬事アソシエエイト・ディレクター
・来年申請予定の製品(希少疾患)の開発薬事責任者
・申請資料~提出のマネージメント
・申請資料作成は、メディカルライターが担当
(変更の範囲)会社の定める業務
■ 応募資格
・3年以上(目安)の医薬品業界での経験(CROの方も可)
・1品目以上の新薬の新薬申請の治験相談(申請の経験不問)
■ 就業場所
(雇入れ直後)東京都
(変更の範囲)会社の定める場所
■ 給与
・現職、経験により考慮
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